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Would This Work: 2,2-dichlorobutane from MEK
what would you get if you did free radicle substitution of malonic acid with excess chlorine ?
woul ... |
4-1-2015 at 09:50
by: CuReUS |
(subsituted) phenol to halobenzene
I came across a very interesting article about making aniline from phenol
[url]http://onlinelibrar ... |
4-1-2015 at 09:44
by: CuReUS |
Druken Aga Challenge (DAC) #3 - Closed (but open to discussion)
[rquote=385011&tid=48085&author=WGTR]
The Birkeland-Eyde route is too expensive on a comme ... |
4-1-2015 at 09:03
by: CuReUS |
dechlorinating 1,4-Dichlorobenzene
[rquote=226571&tid=17894&author=Chemistry Alchemist]Phenol is made by reacting C<sub>6 ... |
2-1-2015 at 01:22
by: CuReUS |
Druken Aga Challenge (DAC) #3 - Closed (but open to discussion)
heating lead nitrate will give NO[sub]2[/sub],but I don't think lead nitrate is OTC
what about do ... |
1-1-2015 at 21:51
by: CuReUS |
Help separating HCl from n-butanol
[rquote=383167&tid=58530&author=HgDinis25]Interesting. The yellow may be the Copper complex ... |
1-1-2015 at 21:45
by: CuReUS |
Benzene synthesis
[rquote=384448&tid=325&author=aga]
You mostly get HCl, Carbon, and a small amount of brown ... |
1-1-2015 at 21:10
by: CuReUS |
Bras ,batteries ,benzene and something in between
[rquote=384417&tid=53527&author=forgottenpassword]If you don't know that it is a reaction wh ... |
1-1-2015 at 21:06
by: CuReUS |
Bras ,batteries ,benzene and something in between
[rquote=384314&tid=53527&author=forgottenpassword]I'm assuming that this is a known reaction ... |
31-12-2014 at 21:55
by: CuReUS |
Bras ,batteries ,benzene and something in between
is there any other way to make ethane 1,2 dithiol instead of the wiki page method
[url]http://en.wi ... |
31-12-2014 at 03:23
by: CuReUS |
the hunt for the reducing agent
[rquote=347543&tid=34833&author=Nicodem]
Do you have a reference for a non-CTH or non-catal ... |
28-12-2014 at 23:54
by: CuReUS |
Reduction of levulinic acid
actually,MPV cannot be done directly on this molecule,because acids kill the aluminum isopropoxide c ... |
28-12-2014 at 23:22
by: CuReUS |
Help separating HCl from n-butanol
[rquote=383065&tid=58530&author=HgDinis25]@CuReUS
It's not tert butanol, it's n-butanol. A ... |
27-12-2014 at 18:32
by: CuReUS |
first acid burn?
[rquote=382689&tid=55708&author=bismuthate]SO3.
It kills (in terms of pain and literally ... |
27-12-2014 at 08:55
by: CuReUS |
N,N-dimethylaniline
actually I am trying to synthesize chloroxylenol ,so i came up with this route
1.p-aminophenol to ... |
27-12-2014 at 08:46
by: CuReUS |
List some BAD chemistry YouTube videos
this video is apt for this thread
all talk,no reaction and a horrible waste of chemicals
they ... |
27-12-2014 at 07:22
by: CuReUS |
Help separating HCl from n-butanol
if you use NaOH to neutralize the HCl,you would have to use a stoichiometric amount or you will end ... |
27-12-2014 at 07:18
by: CuReUS |
N,N-dimethylaniline
I am planning to repeat this reaction ,but on para-aminophenol(from paracetamol) instead as I don' ... |
26-12-2014 at 05:12
by: CuReUS |
Potential route to amphetamine...
instead of reacting methyl iodide with 2- phenylnitroethane ,could simmons smith reaction be done o ... |
21-12-2014 at 05:45
by: CuReUS |
Reducing aliphatic nitro compounds to amines
generally metal reductions are slow ,need a lot of metal,are messy and most of the metal stays unrea ... |
21-12-2014 at 04:43
by: CuReUS |
Organic halides with piperdine
[rquote=379645&tid=54714&author=Dr.Bob]
If you clean your bathroom with Lysol Tub and Tile ... |
19-12-2014 at 05:46
by: CuReUS |
octaazacubane
the idea is very good actually ,that you thought of the nitrogen analogue of cubane
recently i le ... |
18-12-2014 at 01:24
by: CuReUS |
Tired of reporting spam
[rquote=378844&tid=16937&author=gdflp]That would be a lot of work for the mods. [/rquote]
... |
18-12-2014 at 00:51
by: CuReUS |
Organic halides with piperdine
[rquote=379263&tid=54714&author=zed]I'm thinking Dr. Bob might be on the money. Good chanc ... |
18-12-2014 at 00:25
by: CuReUS |
Organic halides with piperdine
[rquote=379214&tid=54714&author=Dr.Bob]piperidines... It is too sterically hindered to for ... |
17-12-2014 at 08:40
by: CuReUS |
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